A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019491



Internal ID18762026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16885894..17358110hg38UCSC Ensembl
Innerchr7:16925518..17397734hg19UCSC Ensembl
Innerchr7:16892043..17364259hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38472217
hg19472217
hg18472217
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6290n100
Supporting Variantsnssv3752908
Samples
Known GenesAHR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019491
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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